All recall categories

Recalls distributed in New Jersey

These notices name New Jersey in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

4,754 stored notices name New Jersey, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.

Medical devices

Reported May 9, 2018

5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length (5 count); Model Number 900-840 Product Usage:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Food

Reported May 9, 2018

Ignite High Endurance Pre-Workout Supplement with Caffeine, brand Back to Health, Net wt. 1 lb. UPC 8 01650 01540 2.…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Independent Nutrition, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 9, 2018

Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Food

Reported May 9, 2018

All dietary supplements manufactured and distributed by Riddhi USA Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Riddhi USA Inc.

FDA (openFDA food enforcement)

Food

Reported May 2, 2018

Formagere de la Brie brand, l 'Explorateur, soft ripened cheese made from pasteurized milk, product comes in a 250g…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Cheezwhse/Com

FDA (openFDA food enforcement)

Medical devices

Reported May 2, 2018

Advance¿ 35LP Low-Profile PTA Balloon Dilatation Catheter; Catalog numbers: PTA5-35-135-6-2 .0 and PTA5-35-135-4-4 .0;…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cook Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

clariti 1 day/Fresh Day 90 pack (-1.00), UV Blocking, 90 silicon hydrogel, daily disposable contact lenses The Clariti…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

CooperVision Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM, Product Number HEM3335, GTIN Number 1 -…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Covidien LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3), Product Code EVT45. Accessory Tips for use only with EVICEL…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ethicon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee system devices are sterile, single-use…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Howmedica Osteonics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Proteus 235, ProteusPLUS or Proteus ONE produces and delivers a proton beam for the treatment of patients with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ion Beam Applications S.A.

FDA (openFDA device enforcement)

Food

Reported May 2, 2018

Shell Eggs packaged in quantities and styles of pack (plastic and pulp cartons, flats, and boxes)

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Rose Acre Farm

FDA (openFDA food enforcement)

Medical devices

Reported May 2, 2018

Versatex Monofilament Mesh 50 x 50cm, Product No. VTX5050M The device is made out of a macroporous three-dimensional…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sofradim Production

FDA (openFDA device enforcement)

Food

Reported Apr 25, 2018

Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Divinity Product Distribution LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 25, 2018

Human Fetal Hemoglobin (HBF-1) FITC Conjugate

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Life Technologies Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 25, 2018

MEVATRON M2 / PRIMUS Mid-Energy, Digital Linear Accelerator, Model No. 01940035 Product Usage: The intended use of the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 25, 2018

SANTA CRUZ organic APRICOT fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10514 8

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Smucker Natural Foods, Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 25, 2018

Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 18, 2018

First aid/emergency kits containing Honeywell eyewash: CSM kit number Kit/cabinet Description CSM Eyewash# Size:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Certified Safety Mfg Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 18, 2018

Refractor Suspension Arm (P/N: 525004, 05 and 525006, 07) The Intended use of this medical device, as part of system to…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Reliance Medical Products Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 18, 2018

Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Magstim Company Limited

FDA (openFDA device enforcement)

Medical devices

Reported Apr 11, 2018

HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

C.R. Bard, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 11, 2018

Wegmans Yogurt Raisins, 9 OZ (255g), in a plastic tub, UPC: 0 77890 31832 4,

High riskUsing this product could cause serious injury, illness or death — stop using it now.

First Source, LLC

FDA (openFDA food enforcement)

Food

Reported Apr 11, 2018

Coconut Smiles - Retail: International Harvest Brand Organic Go Smile! Dried Coconut Raw, in a 9 oz. poly/plastic bag,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

International Harvest, Inc.

FDA (openFDA food enforcement)

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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.